Search Results (3,034)

Groundwater is the main water source for irrigated agriculture, accounting for an increasing share of the domestic supply in the hyper-arid district of La Yarada Los Palos (Tacna, Peru); however, at the sector scale, concerns about arsenic, boron and salinity remain poorly quantified. Arsenic and boron were selected as target contaminants because of their naturally elevated concentrations associated with coastal and volcanic hydrogeological settings, and their well-documented implications for human health and irrigation suitability. This study reports a 12-month monitoring program (September 2024–August 2025) in three irrigated sectors, in which wells were sampled monthly and analyzed by inductively coupled plasma–mass spectrometry (ICP-MS) for total arsenic, boron, lithium and sodium, along with electrical conductivity, pH, temperature and total dissolved solids. The sector–month total arsenic means ranged from 0.0089 to 0.0143 mg L⁻¹, with 33 of 36 exceeding the 0.010 mg L⁻¹ drinking water benchmark recommended by the World Health Organization (WHO). Total boron ranged from 1.11 to 2.76 mg L⁻¹, meaning that all observations were above the 0.5 mg L⁻¹ irrigation guideline for agricultural use proposed by the United Nations Food and Agriculture Organization (FAO). A marked salinity gradient was observed from the inland Sector 1-BH (median Na ≈ 77 mg L⁻¹; EC ≈ 1.2 mS cm⁻¹) to the coastal Sector 3-LC (median Na ≈ 251 mg L⁻¹; EC ≈ 3.3 mS cm⁻¹), with Sector 2-FS showing intermediate salinity but the highest median boron and lithium levels. Spearman rank correlations indicate that sodium, electrical conductivity and total dissolved solids define the main salinity axis, whereas arsenic is only moderately associated with boron and lithium and is not a simple function of bulk salinity. Taken together, these results show that groundwater from the monitored wells is not safe for drinking without treatment and is subject to at least moderate boron-related irrigation restrictions. The sector-resolved dataset provides a quantitative baseline for La Yarada Los Palos and a foundation for future work integrating expanded monitoring, health-risk metrics and management scenarios for arsenic, boron and salinity in hyper-arid coastal aquifers. Full article

Heavy metals are widespread environmental contaminants from natural and anthropogenic sources, posing risks to human health and ecosystems. In urban areas, levels are elevated due to industrial activity, traffic emissions, and building materials. Camden, New Jersey, a city with a history of industry and illegal dumping, faces increased risk due to aging sewer and stormwater systems. These systems frequently flood neighborhoods and parks, heightening residents’ exposure to heavy metals. Despite this, few studies have examined metal distribution in Camden, particularly during storm events. This study analyzes stormwater metal concentrations across residential and commercial areas to assess contamination levels, potential sources, and land use associations. Stormwater samples were collected from 33 flooded street locations after four storm events in summer 2023, along with samples from a flooded residential basement during three storms. All were analyzed for total lead, cadmium, and arsenic using inductively coupled plasma–mass spectrometry (ICP-MS, (Department of Chemistry and Biochemistry, Rowan University, Glassboro, NJ, USA)). Concentration data were visualized using geographic information system (GIS)-based mapping in relation to land use, socioeconomic, and public health factors. In Camden’s stormwater, lead levels (1–1164 µg L⁻¹) were notably higher than those of cadmium (0.1–3.3 µg L⁻¹) and arsenic (0.2–8.6 µg L⁻¹), which were relatively low. Concentrations varied citywide, with localized hot spots shaped by environmental and socio-economic factors. Principal component analysis indicates lead and cadmium likely originate from shared sources, mainly industries and illegal dumping. Notably, indoor stormwater samples showed higher heavy metal concentrations than outdoor street samples, indicating greater exposure risks in flooded homes. These findings highlight the spatial variability and complex sources of heavy metal contamination in stormwater, underscoring the need for targeted interventions in vulnerable communities. Full article

Around eight million people—mainly in cities—die prematurely from pollution-related diseases; thus, studies of urban dust have become increasingly relevant over the last two decades. In this study, an assessment of heavy metal and metalloid contamination in urban dust was conducted in downtown Murcia, Spain. The objectives were to evaluate the level of contamination and the associated health risks, both with a spatially explicit focus. One hundred and twenty-eight urban dust samples were collected, each from a 1-square-meter area, using plastic tools to prevent contamination. The dust was dried and weighed, then acid-digested before analysis via inductively coupled plasma mass spectrometry. Corresponding maps were then generated using a geographic information system. The elements analyzed in the urban dust (with their median concentrations, given in mg/kg) were As (2.14), Bi (14.06), Cd (0.38), Co (1.88), Cr (71.17), Cu (142.60), Fe (13,752), Mn (316.64), Mo (3.90), Ni (21.94), Pb (106.27), Sb (6.54), Se (4.34), Sr (488.08), V (28.05), and Zn (357.33). The sequence of median concentrations for the analyzed elements was Fe > Sr > Zn > Mn > Cu > Pb > Cr > V > Ni > Bi > Sb > Se > Mo > As > Co > Cd. The pollution assessment reveals that the city is moderately polluted. Using local background levels, the elements with median values exceeding the threshold for considerable contamination were As, Cu, Pb, Sb, Se, and Zn. Using the global background level, the elements with median values exceeding the threshold for considerable contamination were Bi, Cu, Mo, Pb, Sb, Se, and Zn. The median value of the sum of the hazard index (1.82) indicates a risk to children’s health. The hazard index revealed that 43% of the sites pose a relative risk to children. In contrast to previous global studies, the present research provides a multi-scale assessment of urban pollution and health risks. Pollution is evaluated by metal, city, zone, and site, while health risks are assessed by metal, city, and site. We recommend a strategy for both local authorities and residents. Full article

To investigate the biosilicification capabilities of Bacillus mucilaginosus and Bacillus polymyxa, silicon concentrations in supernatants from quartz and calcium silicate cultures were monitored over a 12-day period using inductively coupled plasma optical emission spectrometry (ICP-OES). Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) were employed to evaluate changes in the absorption intensity of Si–O–Si characteristic peaks, crystalline phase transformations in the reaction products, and the microstructural morphology of quartz and calcium silicate before and after microbial leaching. The results show that after leaching with B. mucilaginosus, the dissolved silicon concentration in the quartz supernatant reached a maximum of 73.868 mg/L on day 8. In contrast, following treatment with B. polymyxa, the silicon concentration in the calcium silicate supernatant peaked earlier, at 149.153 mg/L on day 4. After microbial leaching, both substrates exhibited marked changes in the intensity of the infrared absorption peaks at 1071 cm⁻¹ and 1083 cm⁻¹, suggesting the formation of Si–O–R type organosilicon complexes. Iron tailings (containing inert silica) and fly ash (containing active silica) were selected for experimental validation. Following treatment with B. mucilaginosus for desilication over an 8-day period, the activity index of iron tailings increased from 77.83% to 90.51%, while that of fly ash rose from 66.32% to 85.01%. ICP-OES analysis confirmed that under the action of B. mucilaginosus, the trends in silicon concentration and activity index in the supernatant of silica-containing solid wastes, such as iron tailings and fly ash, were consistent with those observed in quartz, thereby demonstrating effective biological desilication. These findings provide novel insights into the development of environmentally sound disposal methods for a wider range of solid waste types. Full article

The Sar-e-Sang lapis lazuli deposit has a mining history exceeding 5000 years, producing the world’s finest lapis lazuli. Recently, gem-quality forsterite has been discovered in the marble containing spinel, dolomite, and phlogopite at the periphery of the lapis lazuli ore body at the Pitawak mine, located east of the Sar-e-Sang deposit. The mineral assemblage indicates that the protolith of this marble is dolomite with aluminous and siliceous components. These forsterite crystals occur as colorless, transparent anhedral grains, exhibiting distinct red fluorescence under 365 nm ultraviolet light. To investigate the gemological and spectroscopic characteristics of the Pitawak mine forsterite, this study conducted and analyzed data from basic gemological analysis, electron probe microanalysis (EPMA), Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), ultraviolet–visible absorption spectroscopy (UV-VIS), Fourier-transform infrared spectroscopy (FTIR), laser Raman spectroscopy (RAMAN), and photoluminescence spectroscopy (PL) on four forsterite samples from the Pitawak mine. The analysis results reveal that the samples indicate a composition close to ideal forsterite with a crystal chemical formula of (Mg_2.00Fe_0.02)_Σ2.02Si_0.99O₄. The trace elements present include Fe, Mn, Ca, and minor amounts of Cr and Ni. The UV-VIS spectroscopy results show that the samples possess high transmittance across the visible light range with very weak absorption bands, contributing to the colorless and transparent appearance of Pitawak mine forsterite. This phenomenon is attributed to the extremely low content of chromophoric elements, which have a negligible effect on the forsterite’s color. PL spectroscopy indicates that the red fluorescence of the samples is caused by an emission peak near 642 nm. This emission peak arises from the spin-forbidden ⁴T₁ → ⁶A₁ transition of Mn²⁺ ions situated in octahedral sites within the forsterite structure. Full article

Tiger nut (Cyperus esculentus L.) is a relatively neglected tuber crop with notable nutritional, functional, and ecological value. The primary objective of this study was to evaluate the biological properties and selected nutritional parameters of tiger nut tubers and oil, including antioxidant activity, total phenolic content (TPC), fatty acid (FA) profile, health-related lipid indices, and mineral composition. Methods: Natural and peeled tiger nut tubers, as well as commercially available tiger nut oil (yellow variety, Valencia, Spain), were analyzed. Antioxidant activity was measured spectrophotometrically using the DPPH method. The content of TPC was determined using the Folin–Ciocalteu assay. Fatty acid composition was analyzed by gas chromatography coupled with flame ionization detection, and these data were used to calculate the PUFA/SFA (P/S) ratio, atherogenicity (AI), thrombogenicity (TI) index, and hypocholesterolemic/hypercholesterolemic (h/H) ratio. Macro- and microelement contents were quantified using inductively coupled plasma optical emission spectrometry. Estimated daily intake (EDI), target hazard quotient (THQ), and total THQ (TTHQ) were calculated to assess potential health risks. Results: Natural tiger nut tubers exhibited substantially higher antioxidant activity and TPC compared to peeled tubers, suggesting that the peel is the primary reservoir of phenolic compounds. Strong antioxidant activity was observed in tiger nut oil (64.82 ± 2.59 mg TEAC/L). Oleic acid (C18:1cis n-9) was identified as the predominant FA across all samples, thus contributing positively to favorable health lipid indices (P/S > 0.50, low AI and TI, high h/H ratio). Potassium was the most abundant macroelement in natural and peeled tiger nut tubers. The overall trend of microelement levels in these samples was as follows: Al > Fe > Zn > Cu > Sr > Mn > Li > Ba > Se > As > Cr. All THQ and TTHQ values were below 1, indicating no appreciable health risk associated with consumption. Conclusions: These findings support the use of tiger nuts as a functionally valuable ingredient in health-oriented food products. Full article

Lithium carbonate is one of the most prescribed mood stabilizers worldwide and remains the first-line pharmacological treatment for bipolar disorder (BD). Its therapeutic efficacy is well established; however, lithium (Li) has a narrow therapeutic index, and prolonged or excessive intake can cause renal, neurological, or endocrine toxicity. In Brazil and globally, lithium-based formulations are widely commercialized; however, only Brazil adopts a specific regulatory classification distinguishing reference, generic, and similar medicines. Despite its extensive clinical use, studies monitoring the actual Li concentration in pharmaceutical products are extremely scarce. This study quantified Li concentrations in different formulations available in Brazil to evaluate their chemical uniformity, estimated daily intake, and potential health risks. Samples were digested and analyzed using Inductively Coupled Plasma Optical Emission Spectrometry (ICP OES). Statistical analysis with the Kruskal–Wallis test revealed significant differences among formulations (p = 0.012), confirming non-uniform Li content. Measured concentrations ranged from 245.47 to 315.24 mg/kg, with generic products showing the highest values. The calculated daily intake (DI) and chronic daily intake (CDI) increased with therapeutic dose (600–1800 mg/day), and higher-dose regimens frequently exceeded the permitted daily exposure (PDE) value for Li established by International Council for Harmonisation Guideline for Elemental Impurities (Revision 2) (ICH Q3D (R2) (0.55 mg/day). Moreover, hazard quotient (HQ) values above 1 in some scenarios indicated potential health risks associated with excessive or long-term Li exposure. As one of the first studies to quantify Li in marketed formulations, this work underscores the need for systematic monitoring and stricter quality control to ensure therapeutic safety. Full article

Natural fractures in marine shales are crucial storage spaces and migration pathways for oil and gas, making the study of their formation mechanisms and distribution patterns essential for hydrocarbon exploration and development. This review systematically evaluates the progress in natural fracture studies, transitioning from qualitative to quantitative approaches, with a focus on the genetic mechanisms, distribution patterns, and methodological advancements of fracture types. The review finds that: (1) Integrated “geological-geophysical-dynamic” analyses significantly improve the prediction accuracy of tectonic fracture networks compared to traditional stress-field models. Bedding-parallel fracture development is primarily controlled by the interplay between diagenetic evolution and in situ stress, with their critical opening conditions now being quantifiable; (2) Crucially, the application of micro-scale in situ techniques (e.g., Laser Ablation Inductively Coupled PlasmaMass Spectrometer, laser C-O isotope analysis, carbonate U-Pb dating) has successfully decoded the geochemical signatures and absolute timing of fracture fillings, revealing multiple episodes of fluid activity directly tied to hydrocarbon migration. (3) The combined application of multiple techniques holds promise for deepening the understanding of the coupling mechanisms between fractures. The combined application of these techniques provides a robust framework for deciphering the coupling mechanisms between fracture dynamic evolution and hydrocarbon migration, offering critical insights for future exploration. Full article

Heavy metals (arsenic, cadmium, and lead) remain one of the most common and complex environmental problems worldwide. Accordingly, there is a growing need for eco-friendly and affordable materials derived from agricultural waste for the removal of heavy metals from contaminated water. This study aims to demonstrate how biodegradable pineapple leaf cellulose (PLC) can be used effectively in the remediation of heavy metals. The PLC adsorbent was prepared by treating it with ethyl alcohol (EtOH, 99.5%), calcium chloride (CaCl₂), and 0.8 M sodium hydroxide. A scanning electron microscope equipped with energy-dispersive X-ray spectroscopy (SEM-EDS) and Fourier transform infrared spectroscopy (FT-IR) was used to investigate the surface of the adsorbent. Inductively coupled plasma mass spectrometry (ICP-MS) was employed to measure the concentration of metals before and after adsorption. Removal of metal ions (As⁵⁺, Cd²⁺, and Pb²⁺) by PLC was investigated under varying conditions, including pH, contact time, and adsorbent dosage. The analysis of cellulose composite revealed significant potential for adsorption of heavy metals such as As⁵⁺, Cd²⁺, and Pb²⁺. The highest removal efficiency of heavy metal ions was detected at a pH ranging from 3 to 7. The biosorption order of PLC at pH 6 was Pb²⁺ > Cd²⁺ > As⁵⁺ with 99.53% (63.45 mg/g), 98.44% (37.23 mg/g), and 42.40% (16.27 mg/g), respectively. After 120 min, the equilibrium of the adsorption process was reached for As⁵⁺, Cd²⁺, and Pb²⁺. FT-IR characterization discovered an increased abundance of functional groups on the adsorbent. The SEM-EDS analysis confirmed the occurrence of elements on the surface of PLC. The study revealed that the use of PLC is an innovative method for removing heavy metals from aquatic milieus, a potential resource for eco-friendly and affordable wastewater treatment. Full article

Documenting baseline elemental distribution patterns in crops under non-contaminated conditions provides a physiological reference for understanding constitutive metal homeostasis. This study compared the internal allocation of elements in sunflower (Helianthus annuus), wheat (Triticum aestivum), and maize (Zea mays) grown in soil with a specific geochemical profile. Soil was characterized using X-ray Fluorescence Spectroscopy (XRF) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS). Plants were grown under controlled conditions, and elemental concentrations in roots and shoots were quantified to calculate Bioaccumulation (BCF) and Translocation (TF) Factors. Soil analysis confirmed nickel (42.6 mg kg⁻¹) and copper (32.8 mg kg⁻¹) concentrations within typical global ranges for uncontaminated soils. Species exhibited different distribution tendencies: sunflower showed balanced root–shoot allocation for nickel (TF = 1.00); wheat demonstrated pronounced root retention of nickel and copper (TF < 0.5); and maize exhibited preferential translocation of copper (TF = 0.76) alongside root retention of nickel. Concentrations of lead, selenium, and silver were minimal across all species. The study delineates different species-specific tendencies in internal elemental allocation under given growth conditions. These patterns represent baseline physiological behaviors rather than responses to contamination, providing a comparative dataset that contributes to the understanding of crop ionomics and informs the interpretation of tissue metal concentrations in relation to soil conditions. Full article

Heavy metals release in the environment represents a growing threat to human health and nature, particularly due to industrial activities contributing to soil and water contamination. In this study, Ganoderma lucidum heteropolysaccharides (GLHP) were evaluated as a biosorbent for cadmium removal. The biomass was acquired following the production of Ganoderma lucidum fruiting bodies and consisted of remnants from the fungus and cultivation substrate. Cd(II) and elemental analysis were carried out by atomic adsorption spectrometry (AAS) and inductively coupled plasma mass spectroscopy (ICP-MS), respectively. The biosorption efficiency was critically evaluated, optimizing physical adsorption parameters for batch, column, and percolation configuration, as well as application in real environmental water. Utilizing a simple pre-rinsing step, completely omitting any chemical pretreatment, the Cd(II) removal efficiency was improved from 41.2% to 78.4% in a batch system and up to 98.4% in a fixed-bed column, making it suitable not only for wastewater treatment but also for drinking water purification. The adsorption kinetics were described by a pseudo-second-order (PSO) model and further analyzed using a revised PSO (rPSO) model, which explicitly accounts for adsorbate and adsorbent concentrations. A global fit to the PSO model demonstrated that the rate constant was independent of the adsorbent concentration, supporting its application as a robust descriptor of the adsorption process. GLHP showed good adsorption performance, following the Sips adsorption isotherm and Thomas model for batch and column setup, respectively, demonstrating the potential as a scalable, low-cost biosorbent for fast and efficient Cd(II) removal from contaminated waters. Full article

To fill the gap in systematic data on mineral contents and their dietary contributions in four mainstream dairy products (sterilized, pasteurized, fermented, modified milk) from Henan Province, China, this study aimed to characterize the mineral profiles [magnesium (Mg), iron (Fe), zinc (Zn), selenium (Se), copper (Cu)] and clarify the mineral nutritional disparities between domestic and imported sterilized milk. A total of 150 samples were analysed via inductively coupled plasma mass spectrometry (ICP-MS). Results revealed significant mineral content differences across dairy types: fermented milk had significantly lower Mg and Zn than sterilized and pasteurized milk (p < 0.05). Imported sterilized milk exhibited higher Mg (160.10 ± 31.88 mg/kg) than domestic counterparts (147.41 ± 32.47 mg/kg, p < 0.05). In terms of mineral intake contribution rates (defined as the percentage of mineral intake from dairy products relative to the Recommended Nutrient Intake (RNI), unit: %), the rates are ranked in descending order as follows: Se (11.68–25.32%) > Mg (11.11–20.76%) > Zn (5.88–16.33%) > Cu (0.62–1.81%) > Fe (0.25–1.00%). This study elucidates the mineral profiles of Henan’s dairy products, supporting residents’ dairy choices and optimisation of dairy processing technologies. Full article

Early exposure to toxic metals is a growing concern due to its potential neurodevelopmental effects in children. This study investigates whether exposure to multiple metals during pregnancy influences early developmental outcomes in children aged 12–18 months living in a metropolitan setting. We conducted a prospective cohort study in Rio de Janeiro that included 393 children from PIPA project. Umbilical cord blood samples obtained at birth were processed using ICP-MS (Inductively Coupled Plasma Mass Spectrometry) to quantify metals (arsenic, lead and mercury). The children’s neurodevelopment was assessed with the Denver-II tool. We applied logistic regression analyses to explore the relationship between metal concentrations and developmental outcomes, controlling for possible confounding variables. Higher prenatal arsenic levels were linked to poorer gross motor performance, both in continuous models (OR = 1.65; 95% CI: 1.09–2.51) and in subjects with concentrations above the 95th percentile (OR = 8.84; 95% CI: 2.40–32.61), this was consistent across multi-metal models. A negative relationship between Pb concentrations and gross motor delays was observed, with an estimated Odds Ratio of 0.49 (95% CI: 0.24–0.98). Hg exposure demonstrated no association with neurodevelopment in any model. However, the lack of postnatal arsenic exposure data limits the distinction between prenatal and early childhood effects. These findings underscore the need for the continued monitoring and investigation of combined metal exposures during pregnancy. Future studies integrating prenatal and postnatal exposure assessments are warranted. Full article

Monitoring trace metals in commercially important fish species provides an early warning of anthropogenic contamination and potential risk to consumers. This study semi-quantified and quantified essential, non-essential, and toxic elements in the muscle of wild meagre (Argyrosomus regius) captured in the Tagus estuary (Portugal), which is used as a nursery and spawning aggregation area. Dry muscle was microwave-digested and analyzed using inductively coupled plasma–optical emission spectroscopy. Semi-quantified screening detected Al, B, Ca, Fe, K, Mg, Na, P, S, Si, Sr, and Ti, and eight elements were determined using multielement calibration (As, Cr, Cu, Hg, Mn, Ni, Se, and Zn); Cd, Pb (toxic elements), Co, and Mo were not detected in this study. Arsenic was detected in all individuals, with a minimum value of 0.348 mg/kg wet weight. A mercury level above the European Commission regulatory limit (0.5 mg/kg wet weight) was only detected in one individual, corresponding to 2% of the samples. Although other metals remain well below regulatory limits, continued biomonitoring is recommended to track temporal trends and safeguard seafood safety in transitional coastal systems, which is important for commercially relevant fish species. Full article

Iodine deficiency is the leading preventable cause of neurological damage worldwide. Dairy foods represent an important dietary iodine source. This study aimed to assess iodine concentration in milk, ricotta cheese, and yogurt, and to evaluate their contribution toward the recommended daily iodine intake. Whole pasteurized milk (WM; n = 12), partially skimmed pasteurized milk (PM; n = 21), skimmed pasteurized milk (SM; n = 7), ricotta cheese (RC; n = 26), whole yogurt (WY; n = 13), and low-fat yogurt (LY; n = 15) were purchased in local stores. Samples were analyzed through inductively coupled plasma mass spectrometry for iodine quantification. After removing outliers, the final dataset comprised 11 WM, 19 PM, 7 SM, 26 RC, 13 WY and 15 LY samples. Data were investigated through a mixed model with iodine concentration as the dependent variable, product type as fixed effect, and brand as random effect. Low-fat yogurt exhibited the greatest estimated iodine concentration (293.76 µg/kg), while SM and WM exhibited the lowest (211.92 and 197.63 µg/kg, respectively). Based on these results, a serving of milk (250 g) would provide 31.82–39.08% of the average daily iodine requirement, a serving of ricotta (125 g) 21.66%, and a yogurt jar (125 g) 21.54–24.11%. These findings confirm the nutritional relevance of dairy products as primary iodine sources. Full article